Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,041 recalls have been distributed to Louisiana in the last 12 months.
Showing 16461–16480 of 51,202 recalls
Recalled Item: BD UF PEN 32GX4MM 100 NANO Item Number: 4292272 Recalled by Cardinal Health...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VAPORIZER VICKS 1.5GAL Item Number: 2354942 Recalled by Cardinal Health Inc....
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 35" (89 cm) Appx 3.9 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXCOM G6 SENSOR 3 PACK Item Number: 5447552 Recalled by Cardinal Health...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877 Recalled...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port Recalled by...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 40" (102 cm) Appx. 4.8 ml Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Controller - Product Usage: intended for use with a Recalled by Boston...
The Issue: May have been programmed with a less than optimal brightness setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 1.0 ml Recalled by ICU Medical, Inc. Due to Due to molding defect,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 4.1 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....
The Issue: BBMI has identified through complaints the potential for the extension set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...
The Issue: Possible false negative or false positive results due to the product being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.